nstd133 (Redin et al. 2016)
- Organism:
- Human
- Study Type:
- Case-Set
- Submitter:
- Claire Redin
- Description:
- Detailed breakpoint mapping of 248 balanced chromosomal rearrangements at nucleotide resolution using sequencing in subjects with congenital anomalies, based on initially provided karyotpes. See Variant Summary counts for nstd133 in dbVar Variant Summary.
- Curatorial Comment:
- PLEASE NOTE: All clinical variants in dbVar (including the variants in this study) have been re-accessioned in the study Clinical Structural Variants (nstd102). The new accessions are preferred and will be kept up to date with changes made in ClinVar. We recommend using the new nstd102 accessions whenever possible. A file mapping old accessions to new is available at https://ftp.ncbi.nlm.nih.gov/pub/dbVar/data/release_notes/nstd102_accession_mapping.txt.
- Publication(s):
- Redin et al. 2016
- Last updated:
- 2016-09-15
Detailed Information: Download 246 Variant Regions, Download 921 Variant Calls, Download Both, FTP
Variant Summary
Assembly used for analysis:
Remapped: GRCh38.p12 (hg38)
Submitted: GRCh37 (hg19)
Sequence ID | Chr | Number of Variant Regions | Number of Variant Calls | Placement type | Link to graphical display |
---|---|---|---|---|---|
NC_000001.11 | Chr1 | 38 | 93 | Remapped | NC_000001.11 |
NC_000002.12 | Chr2 | 49 | 154 | Remapped | NC_000002.12 |
NC_000003.12 | Chr3 | 27 | 62 | Remapped | NC_000003.12 |
NC_000004.12 | Chr4 | 18 | 55 | Remapped | NC_000004.12 |
NC_000005.10 | Chr5 | 36 | 126 | Remapped | NC_000005.10 |
NC_000006.12 | Chr6 | 32 | 164 | Remapped | NC_000006.12 |
NC_000007.14 | Chr7 | 31 | 92 | Remapped | NC_000007.14 |
NC_000008.11 | Chr8 | 14 | 43 | Remapped | NC_000008.11 |
NC_000009.12 | Chr9 | 21 | 87 | Remapped | NC_000009.12 |
NC_000010.11 | Chr10 | 20 | 60 | Remapped | NC_000010.11 |
NC_000011.10 | Chr11 | 18 | 47 | Remapped | NC_000011.10 |
NC_000012.12 | Chr12 | 17 | 41 | Remapped | NC_000012.12 |
NC_000013.11 | Chr13 | 14 | 32 | Remapped | NC_000013.11 |
NC_000014.9 | Chr14 | 28 | 76 | Remapped | NC_000014.9 |
NC_000015.10 | Chr15 | 10 | 23 | Remapped | NC_000015.10 |
NC_000016.10 | Chr16 | 12 | 29 | Remapped | NC_000016.10 |
NC_000017.11 | Chr17 | 15 | 37 | Remapped | NC_000017.11 |
NC_000018.10 | Chr18 | 13 | 53 | Remapped | NC_000018.10 |
NC_000019.10 | Chr19 | 9 | 19 | Remapped | NC_000019.10 |
NC_000020.11 | Chr20 | 9 | 28 | Remapped | NC_000020.11 |
NC_000021.9 | Chr21 | 5 | 12 | Remapped | NC_000021.9 |
NC_000022.11 | Chr22 | 6 | 13 | Remapped | NC_000022.11 |
NC_000023.11 | ChrX | 26 | 67 | Remapped | NC_000023.11 |
NC_000024.10 | ChrY | 2 | 4 | Remapped | NC_000024.10 |
NW_017363813.1 | Chr3|NW_017363813.1 | 1 | 2 | Remapped | NW_017363813.1 |
NW_019805488.1 | Chr3|NW_019805488.1 | 1 | 2 | Remapped | NW_019805488.1 |
NT_187544.1 | Chr4|NT_187544.1 | 1 | 1 | Remapped | NT_187544.1 |
NW_003315914.1 | Chr4|NW_003315914.1 | 1 | 2 | Remapped | NW_003315914.1 |
NW_013171801.1 | Chr4|NW_013171801.1 | 1 | 2 | Remapped | NW_013171801.1 |
NT_187548.1 | Chr5|NT_187548.1 | 1 | 2 | Remapped | NT_187548.1 |
NT_187651.1 | Chr5|NT_187651.1 | 1 | 2 | Remapped | NT_187651.1 |
NT_187556.1 | Chr6|NT_187556.1 | 3 | 6 | Remapped | NT_187556.1 |
NW_003315921.1 | Chr6|NW_003315921.1 | 1 | 2 | Remapped | NW_003315921.1 |
NW_012132918.1 | Chr6|NW_012132918.1 | 1 | 2 | Remapped | NW_012132918.1 |
NT_187563.1 | Chr7|NT_187563.1 | 1 | 2 | Remapped | NT_187563.1 |
NW_009646202.1 | Chr10|NW_009646202.1 | 1 | 2 | Remapped | NW_009646202.1 |
NT_187586.1 | Chr11|NT_187586.1 | 1 | 2 | Remapped | NT_187586.1 |
NW_018654718.1 | Chr12|NW_018654718.1 | 1 | 2 | Remapped | NW_018654718.1 |
NT_187614.1 | Chr17|NT_187614.1 | 1 | 1 | Remapped | NT_187614.1 |
NT_187615.1 | Chr17|NT_187615.1 | 1 | 2 | Remapped | NT_187615.1 |
NW_003315954.1 | Chr17|NW_003315954.1 | 1 | 2 | Remapped | NW_003315954.1 |
NW_017363819.1 | Chr17|NW_017363819.1 | 1 | 2 | Remapped | NW_017363819.1 |
NW_014040928.1 | Chr18|NW_014040928.1 | 1 | 2 | Remapped | NW_014040928.1 |
NW_014040929.1 | Chr19|NW_014040929.1 | 1 | 2 | Remapped | NW_014040929.1 |
Sequence ID | Chr | Number of Variant Regions | Number of Variant Calls | Placement type | Link to graphical display |
---|---|---|---|---|---|
NC_000001.10 | Chr1 | 38 | 93 | Submitted | NC_000001.10 |
NC_000002.11 | Chr2 | 49 | 154 | Submitted | NC_000002.11 |
NC_000003.11 | Chr3 | 27 | 62 | Submitted | NC_000003.11 |
NC_000004.11 | Chr4 | 18 | 55 | Submitted | NC_000004.11 |
NC_000005.9 | Chr5 | 36 | 126 | Submitted | NC_000005.9 |
NC_000006.11 | Chr6 | 32 | 164 | Submitted | NC_000006.11 |
NC_000007.13 | Chr7 | 31 | 92 | Submitted | NC_000007.13 |
NC_000008.10 | Chr8 | 14 | 43 | Submitted | NC_000008.10 |
NC_000009.11 | Chr9 | 21 | 87 | Submitted | NC_000009.11 |
NC_000010.10 | Chr10 | 20 | 60 | Submitted | NC_000010.10 |
NC_000011.9 | Chr11 | 18 | 47 | Submitted | NC_000011.9 |
NC_000012.11 | Chr12 | 17 | 41 | Submitted | NC_000012.11 |
NC_000013.10 | Chr13 | 14 | 32 | Submitted | NC_000013.10 |
NC_000014.8 | Chr14 | 28 | 76 | Submitted | NC_000014.8 |
NC_000015.9 | Chr15 | 10 | 23 | Submitted | NC_000015.9 |
NC_000016.9 | Chr16 | 12 | 29 | Submitted | NC_000016.9 |
NC_000017.10 | Chr17 | 15 | 37 | Submitted | NC_000017.10 |
NC_000018.9 | Chr18 | 13 | 53 | Submitted | NC_000018.9 |
NC_000019.9 | Chr19 | 9 | 19 | Submitted | NC_000019.9 |
NC_000020.10 | Chr20 | 9 | 28 | Submitted | NC_000020.10 |
NC_000021.8 | Chr21 | 5 | 12 | Submitted | NC_000021.8 |
NC_000022.10 | Chr22 | 6 | 13 | Submitted | NC_000022.10 |
NC_000023.10 | ChrX | 26 | 67 | Submitted | NC_000023.10 |
NC_000024.9 | ChrY | 2 | 4 | Submitted | NC_000024.9 |
Variant Region remap status | Variant Call remap status | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Sequence ID | Chr | Variant Regions on source | Perfect | Good | Pass | Fail | Mult | Variant Calls on source | Perfect | Good | Pass | Fail | Mult |
NC_000001.10 | Chr1 | 38 | 0 | 0 | 0 | 0 | 228 | 93 | 0 | 0 | 0 | 0 | 228 |
NC_000002.11 | Chr2 | 49 | 0 | 0 | 0 | 0 | 394 | 154 | 0 | 0 | 0 | 0 | 394 |
NC_000003.11 | Chr3 | 27 | 0 | 0 | 0 | 0 | 136 | 62 | 0 | 0 | 0 | 0 | 136 |
NC_000004.11 | Chr4 | 18 | 0 | 0 | 0 | 0 | 132 | 55 | 0 | 0 | 0 | 0 | 132 |
NC_000005.9 | Chr5 | 36 | 0 | 0 | 0 | 0 | 344 | 126 | 0 | 0 | 0 | 0 | 344 |
NC_000006.11 | Chr6 | 32 | 0 | 0 | 0 | 0 | 516 | 164 | 0 | 0 | 0 | 0 | 516 |
NC_000007.13 | Chr7 | 31 | 0 | 0 | 0 | 0 | 242 | 92 | 0 | 0 | 0 | 0 | 242 |
NC_000008.10 | Chr8 | 14 | 0 | 0 | 0 | 0 | 104 | 43 | 0 | 0 | 0 | 0 | 104 |
NC_000009.11 | Chr9 | 21 | 0 | 0 | 0 | 0 | 264 | 87 | 0 | 0 | 0 | 0 | 264 |
NC_000010.10 | Chr10 | 20 | 0 | 0 | 0 | 0 | 156 | 60 | 0 | 0 | 0 | 0 | 156 |
NC_000011.9 | Chr11 | 18 | 0 | 0 | 0 | 0 | 112 | 47 | 0 | 0 | 0 | 0 | 112 |
NC_000012.11 | Chr12 | 17 | 0 | 0 | 0 | 0 | 104 | 41 | 0 | 0 | 0 | 0 | 104 |
NC_000013.10 | Chr13 | 14 | 0 | 0 | 0 | 0 | 72 | 32 | 0 | 0 | 0 | 0 | 72 |
NC_000014.8 | Chr14 | 28 | 0 | 0 | 0 | 0 | 184 | 76 | 0 | 0 | 0 | 0 | 184 |
NC_000015.9 | Chr15 | 10 | 0 | 0 | 0 | 0 | 52 | 23 | 0 | 0 | 0 | 0 | 52 |
NC_000016.9 | Chr16 | 12 | 0 | 0 | 0 | 0 | 60 | 29 | 0 | 0 | 0 | 0 | 60 |
NC_000017.10 | Chr17 | 15 | 0 | 0 | 0 | 0 | 86 | 37 | 0 | 0 | 0 | 0 | 86 |
NC_000018.9 | Chr18 | 13 | 0 | 0 | 0 | 0 | 138 | 53 | 0 | 0 | 0 | 0 | 138 |
NC_000019.9 | Chr19 | 9 | 0 | 0 | 0 | 0 | 40 | 19 | 0 | 0 | 0 | 0 | 40 |
NC_000020.10 | Chr20 | 9 | 0 | 0 | 0 | 0 | 64 | 28 | 0 | 0 | 0 | 0 | 64 |
NC_000021.8 | Chr21 | 5 | 0 | 0 | 0 | 0 | 24 | 12 | 0 | 0 | 0 | 0 | 24 |
NC_000022.10 | Chr22 | 6 | 0 | 0 | 0 | 0 | 28 | 13 | 0 | 0 | 0 | 0 | 28 |
NC_000023.10 | ChrX | 26 | 0 | 0 | 0 | 0 | 196 | 67 | 0 | 0 | 0 | 0 | 196 |
NC_000024.9 | ChrY | 2 | 0 | 0 | 0 | 0 | 8 | 4 | 0 | 0 | 0 | 0 | 8 |
Samplesets
Number of Samplesets: 1
- Name:
- Mapped_BCAs
- Description:
- 248 sucessfully mapped rearrangements
- Size:
- 248
- Organisms:
- Homo sapiens
- Sampleset Phenotype(s):
- Abnormality of prenatal development or birth
Neurodevelopmental abnormality
Phenotypic abnormality
Experimental Details
Experiment ID | Type | Method | Analysis | Number of Variant Calls |
---|---|---|---|---|
1 | Discovery | Sequencing | Split read and paired-end mapping | 755 |
2 | Discovery | Sequencing | Split read mapping | 83 |
3 | Discovery | Sequencing | Split read and paired-end mapping | 66 |
4 | Discovery | Merging of experiments 1,2 | Merging of experiments 1,2 | 17 |